FDAMay 11, 2026device

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

What to do

FDA enforcement status: Completed

Brands named

boston scientificboston

UPCs

00850014110147

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device — Recall Details · AllClear